| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs764969 | snp | G/T | 0 | 0 | intron-variant | HERC6 | GRCh38.p7 | 4:88409363 | agaaatctgacatgg[G/T]tgactctatcttgct | 55008 |
| rs764970 | snp | G/T | 0.00523557 | 0.0508957 | intron-variant | HERC6 | GRCh38.p7 | 4:88409433 | TCATAATGAACACTA[G/T]CCCCCTCTTTCGGCC | 55008 |
| rs1025808 | snp | A/T | 0 | 0 | intron-variant | HERC6 | GRCh38.p7 | 4:88395195 | AATTGTTTGGATTAT[A/T]TTATTCTCAATATAA | 55008 |
| rs1025809 | snp | A/G | 0.215747 | 0.247642 | intron-variant | HERC6 | GRCh38.p7 | 4:88395614 | tcatatatgaaacac[A/G]ttattaactatagtc | 55008 |
| rs1025810 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HERC6 | GRCh38.p7 | 4:88395793 | ccttccaaagtgctg[G/T]tattacaggtgtgag | 55008 |
| rs1025811 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | HERC6 | GRCh38.p7 | 4:88396306 | TTTAATCTTTATTCT[A/G]Gatattttatttatt | 55008 |
| rs1059339 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88415442 | GGGTGATATGATGAC[C/T]TTGACTCTGTGGAGG | 55008 |
| rs1866798 | snp | A/C | 0.484561 | 0.0864924 | intron-variant | HERC6 | GRCh38.p7 | 4:88390264 | acatcttctgatttc[A/C]ccccaacccccagcc | 55008 |
| rs2119321 | snp | C/T | 0.324855 | 0.23853 | intron-variant | HERC6 | GRCh38.p7 | 4:88388481 | TCACTGCAACCTCTG[C/T]CTCCCAGGATCAAGT | 55008 |
| rs2119322 | snp | C/T | 0.355311 | 0.226737 | intron-variant | HERC6 | GRCh38.p7 | 4:88392830 | CATGTGTACTGGCCA[C/T]TGCTAGAAGAGCGTC | 55008 |
| rs2165335 | snp | A/C | | | intron-variant | HERC6 | GRCh38.p7 | 4:88395216 | CTCAATATAAAGAAT[A/C]AATAGAAATAAATAG | 55008 |
| rs2582037 | snp | C/G | | | | | GRCh38.p7 | 4:88390689 | CCCCAAGCCCAGCTG[C/G]CCATGGCTGTTCTTT | 55008 |
| rs2582038 | snp | C/T | 0.0539704 | 0.155153 | | | GRCh38.p7 | 4:88385354 | TATAGTACCTTTATT[C/T]CAAAGCCCTCAAACT | 55008 |
| rs3806784 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88423774 | TTCTTCTTATCTGTA[C/T]AACAGCCATACATAT | 55008 |
| rs4298105 | snp | A/G | 0 | 0 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88429806 | TATGTCTCCCTTCAT[A/G]CCTATTTTTCTTTAA | 55008 |
| rs4365686 | snp | C/T | 0.498693 | 0.0255257 | intron-variant, upstream-variant-2KB | HERC6, LOC102723458 | GRCh38.p7 | 4:88424935 | TTATTTCTGGTTGTC[C/T]TACTCGTGTTCACTG | 55008 |
| rs4413373 | snp | C/T | 0.00603186 | 0.0545852 | stop-gained, nc-transcript-variant, intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88442452 | TCACCCATGCTCACA[C/T]AGTCATAATCACCTC | 55008 |
| rs4498108 | snp | A/G | 0.362941 | 0.223034 | intron-variant | HERC6 | GRCh38.p7 | 4:88383620 | ACAAGAAAATTAGCC[A/G]GGCATGGTGTCAGGC | 55008 |
| rs4524346 | snp | A/G/T | 0.00755907 | 0.0610114 | intron-variant | HERC6 | GRCh38.p7 | 4:88406803 | tcactctgtcaccca[A/G/T]gccggagtgcagtag | 55008 |
| rs4693958 | snp | G/T | 0.499673 | 0.0127754 | intron-variant | HERC6 | GRCh38.p7 | 4:88395713 | AATTTGTGTAGAGAT[G/T]GGGTCTTGCTATATT | 55008 |
| rs5025386 | snp | A/T | 0.216649 | 0.247765 | intron-variant | HERC6 | GRCh38.p7 | 4:88395696 | ATGATTTTTTTTTTT[A/T]AAATTTGTGTAGAGA | 55008 |
| rs5860132 | in-del | -/C | 0.394538 | 0.203982 | intron-variant | HERC6 | GRCh38.p7 | 4:88389708 | GGGATACTTTAATCT[-/C]ATTTTTTTCTTCATC | 55008 |
| rs5860133 | in-del | -/A | 0.498964 | 0.02274 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88417948 | AAAACCACATTTCTT[-/A]AAAAAAAAAAAAAGT | 55008 |
| rs6532067 | snp | A/G | 0.210605 | 0.246877 | intron-variant | HERC6 | GRCh38.p7 | 4:88383724 | TGCTGGGACAGCGCC[A/G]CTGCACTCCAGCCTG | 55008 |
| rs6532068 | snp | C/T | 0.0166966 | 0.0898305 | intron-variant, missense, nc-transcript-variant, upstream-variant-2KB | HERC6, LOC102723458 | GRCh38.p7 | 4:88424608 | AGATACCTGCAGAAA[C/T]CCCCAGTCCTGTTAT | 55008 |
| rs6825220 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HERC6 | GRCh38.p7 | 4:88403791 | aaataaaaaaaaTTT[A/T]AAAAAGGaacccaga | 55008 |
| rs6825412 | snp | A/T | 0.49907 | 0.0215454 | intron-variant | HERC6 | GRCh38.p7 | 4:88403872 | acaatttgccatttt[A/T]atcattttaagtata | 55008 |
| rs6841213 | snp | A/T | 0.490563 | 0.0680388 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88416446 | ttaggctattaaaaa[A/T]ttttttttactttgt | 55008 |
| rs6849574 | snp | G/T | 0 | 0 | intron-variant | HERC6 | GRCh38.p7 | 4:88388096 | GAGATATGTTAGCAT[G/T]TCACTGGGTATATAC | 55008 |
| rs6850385 | snp | C/T | 0.486133 | 0.082104 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88414515 | gtgaaagtaagttta[C/T]taagaaagtagaaga | 55008 |
| rs6854823 | snp | C/G | 0.498734 | 0.0251279 | intron-variant | HERC6 | GRCh38.p7 | 4:88397303 | TTTTAGTAGAGATGG[C/G]GTTTCTCCGTGTTGG | 55008 |
| rs7438209 | snp | G/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88406875 | tattctcctgcctca[G/T]cctcctgaatagctg | 55008 |
| rs7439793 | snp | A/C | 0 | 0 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88426059 | ATTTTCCAATGTGCC[A/C]TGCCCCATAAATCCA | 55008 |
| rs7660771 | snp | A/G | 0.209693 | 0.246729 | intron-variant | HERC6 | GRCh38.p7 | 4:88383910 | GTGAAATGAGATGTG[A/G]CCCTTTGATCTTAAT | 55008 |
| rs7662660 | snp | A/G | 0.267636 | 0.249377 | intron-variant | HERC6 | GRCh38.p7 | 4:88399254 | TGTGGTCAGAGGCAA[A/G]GGTTTCTGTGCTGTT | 55008 |
| rs7663920 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88420749 | ccagcctgggcaaca[C/T]agtgagaccttgtct | 55008 |
| rs7670637 | snp | C/T | 0.497359 | 0.0362457 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88421824 | agtgggaaatgatat[C/T]tccttgtgattttga | 55008 |
| rs7677237 | snp | C/T | 0.124277 | 0.216087 | missense, utr-variant-5-prime, nc-transcript-variant | HERC6 | GRCh38.p7 | 4:88385507 | ATTATAGGAAAATAA[C/T]GACTCTGAATGATAT | 55008 |
| rs7678100 | snp | A/G | 0.136847 | 0.222927 | intron-variant | HERC6 | GRCh38.p7 | 4:88389215 | GTCTTGAGAGGAGTG[A/G]GCAGGGGGAGATGAA | 55008 |
| rs7685901 | snp | A/C | 0.181659 | 0.240478 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88420851 | gtataacctttaccc[A/C]aatcaactttacaac | 55008 |
| rs7686081 | snp | A/C | 0.182296 | 0.240658 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88420850 | tgtataacctttacc[A/C]aaatcaactttacaa | 55008 |
| rs10003728 | snp | A/G | 0.456214 | 0.141336 | upstream-variant-2KB | HERC6 | GRCh38.p7 | 4:88377049 | AAAAGTTAGCTGGGC[A/G]TAGTGGCACGTGCCT | 55008 |
| rs10006830 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88433951 | GGTGTGCCAATGGTA[C/T]GATTTTTTGTTGGTC | 55008 |
| rs10008548 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | HERC6 | GRCh38.p7 | 4:88388198 | agcactctggaaggg[C/G]atcacttgaggccag | 55008 |
| rs10015822 | snp | C/T | 0.438806 | 0.163867 | intron-variant | HERC6 | GRCh38.p7 | 4:88380522 | aggaaatcgagacca[C/T]cctggccaatatgat | 55008 |
| rs10016660 | snp | A/G | 0.331642 | 0.236293 | intron-variant | HERC6 | GRCh38.p7 | 4:88409137 | AATTGGGGAAGTTGC[A/G]AATCTTATGACCTCC | 55008 |
| rs10030059 | snp | C/G | 0.49753 | 0.0350569 | intron-variant | HERC6 | GRCh38.p7 | 4:88400615 | tcataaattttaaat[C/G]acatgttctgggtgg | 55008 |
| rs10030171 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | HERC6 | GRCh38.p7 | 4:88400731 | agacaggggcaccac[A/G]tttacatatgtttta | 55008 |
| rs10433947 | snp | A/T | 0.34146 | 0.23267 | intron-variant | HERC6 | GRCh38.p7 | 4:88386372 | caccatgcccggcta[A/T]tttttgtatttttag | 55008 |
| rs10516807 | snp | A/G | 0.0496527 | 0.149536 | intron-variant | HERC6 | GRCh38.p7 | 4:88398078 | TAAATTTTTGGCTTG[A/G]TAATACATCAGATTT | 55008 |
| rs10670260 | in-del | -/AT | | | intron-variant | HERC6 | GRCh38.p7 | 4:88379687 | TATAAATATATACAA[-/AT]ATATATAATATATAA | 55008 |
| rs10707148 | in-del | -/T | 0.158962 | 0.232835 | intron-variant | HERC6 | GRCh38.p7 | 4:88388148 | TAAGCTTAGATTAGA[-/T]TTTTTTTTTCTGGCT | 55008 |
| rs11097187 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | HERC6 | GRCh38.p7 | 4:88380949 | tatgcaactctgtac[A/G]ttgtgttttcatcaa | 55008 |
| rs11392030 | in-del | -/G | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | HERC6 | GRCh38.p7 | 4:88379097 | TCAGCTGGGCCGCAG[-/G]GGCGCGCAGCGCGGG | 55008 |
| rs11942136 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | HERC6 | GRCh38.p7 | 4:88392419 | ggttttgaactcctg[C/T]gctcaagtgatccac | 55008 |
| rs11942237 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HERC6 | GRCh38.p7 | 4:88392460 | ctcccaaagcactgg[A/G]attacaggtgtgaga | 55008 |
| rs11946811 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | HERC6 | GRCh38.p7 | 4:88397672 | GCCTGGGCAACAGGG[C/T]GAGACTCCATCTCAA | 55008 |
| rs12501863 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | HERC6 | GRCh38.p7 | 4:88398810 | GTCAGGCAGCAATCG[A/G]AGTTCTTCAAATGGA | 55008 |
| rs12504318 | snp | A/G | 0.114387 | 0.210022 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88418391 | cttaggacaagccca[A/G]cttgatgagtagatg | 55008 |
| rs12505850 | snp | A/C | 0.093417 | 0.194889 | intron-variant, upstream-variant-2KB | HERC6, LOC102723458 | GRCh38.p7 | 4:88438025 | GTAGTCTCAGCTACT[A/C]AGGAGGCTGAGGATT | 55008 |
| rs12510688 | snp | C/T | 0.174565 | 0.238347 | missense, utr-variant-5-prime, nc-transcript-variant | HERC6 | GRCh38.p7 | 4:88390810 | TTTGCCCTGTCTCTC[C/T]GTGGGACTTCGTTTG | 55008 |
| rs12640868 | snp | G/T | 0.00943375 | 0.0680285 | intron-variant | HERC6 | GRCh38.p7 | 4:88403895 | taagtatacaattta[G/T]tgacagtgacattaa | 55008 |
| rs12641463 | snp | C/G | 0.256061 | 0.249927 | intron-variant | HERC6 | GRCh38.p7 | 4:88409898 | CTTAGTGCTCAGGAT[C/G]CTGTAGACTGGGTAG | 55008 |
| rs12641473 | snp | C/G | 0.254944 | 0.249951 | intron-variant | HERC6 | GRCh38.p7 | 4:88410079 | ATATCTAAGACAGGT[C/G]TCAGTTAATTTAGAA | 55008 |
| rs12642398 | snp | C/T | 0.499767 | 0.0107802 | intron-variant | HERC6 | GRCh38.p7 | 4:88402062 | gctgggtaaggagga[C/T]gaaagagggtgatga | 55008 |
| rs12642811 | snp | C/T | 0.0152663 | 0.0860237 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88416537 | tttattctatggttt[C/T]tggatttggggtcat | 55008 |
| rs12650077 | snp | C/T | 0 | 0 | intron-variant | HERC6 | GRCh38.p7 | 4:88405905 | TATACAAAGGATCGG[C/T]TAAATCTCACATTGC | 55008 |
| rs12651181 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HERC6 | GRCh38.p7 | 4:88401835 | CATTAgacaatatca[C/G]gtgcccatttgaaat | 55008 |
| rs13136579 | snp | A/C | | | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88417906 | agctatgattgtgcc[A/C]ctgtaccccagcctg | 55008 |
| rs13138145 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88435531 | GAACTATCAATTTGT[A/G]TTCAAAATTATGGAA | 55008 |
| rs13142699 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88381581 | tttttttttttgaga[A/T]ggggttttgccctgt | 55008 |
| rs13150730 | snp | A/T | | | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88440719 | gaggtggaaccccca[A/T]ggtggacatgcctgg | 55008 |
| rs17014114 | snp | C/T | 0.226188 | 0.248863 | intron-variant | HERC6 | GRCh38.p7 | 4:88393158 | GGAAGATTAGATAGC[C/T]TCCAGAAATAAATGT | 55008 |
| rs17014115 | snp | A/G | 0.338069 | 0.233974 | intron-variant | HERC6 | GRCh38.p7 | 4:88395077 | GGAGCCATAAGGAAT[A/G]GACTTGAAAACTACT | 55008 |
| rs17014118 | snp | C/T | 0.49427 | 0.0532195 | missense, utr-variant-5-prime, nc-transcript-variant | HERC6 | GRCh38.p7 | 4:88398144 | GACTTTCTTTTAGAC[C/T]TCGTGGATGTTCAAG | 55008 |
| rs17014122 | snp | C/G | 0.258565 | 0.249853 | intron-variant | HERC6 | GRCh38.p7 | 4:88398582 | GGTTTCTGACATGTC[C/G]TGGAGGGAATTTCCC | 55008 |
| rs17014129 | snp | C/T | 0.114387 | 0.210022 | intron-variant | HERC6 | GRCh38.p7 | 4:88402942 | GGGAACTTTAAGAGC[C/T]GTGGTTACCTGTCTT | 55008 |
| rs17014130 | snp | G/T | 0.0908922 | 0.192833 | intron-variant | HERC6 | GRCh38.p7 | 4:88405456 | ATTTTCATTAATAAT[G/T]ATTCCACGTCATCAT | 55008 |
| rs17014132 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | HERC6 | GRCh38.p7 | 4:88408425 | CTTTAAGAAAAAGGT[C/T]TGTATCTTATATGTA | 55008 |
| rs17014133 | snp | A/G | 0.029116 | 0.117091 | intron-variant, nc-transcript-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88415589 | AATATCGGTCTGCAT[A/G]CTTTCCAACCATGTT | 55008 |
| rs17014135 | snp | A/G | 0.141934 | 0.225437 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88441604 | ATGACTTCTCTCACC[A/G]TCTCATCCCATTTGT | 55008 |
| rs17790863 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HERC6 | GRCh38.p7 | 4:88395339 | AACCTCATACTTAAA[C/T]GTTGGTTTTACTCTT | 55008 |
| rs17790893 | snp | A/G | 0.275197 | 0.248727 | intron-variant | HERC6 | GRCh38.p7 | 4:88395357 | TGGTTTTACTCTTGA[A/G]CCAGTTAATTTATCT | 55008 |
| rs28368727 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HERC6 | GRCh38.p7 | 4:88382673 | AACATTCAGCAGTTC[A/G]TGAATTGAGCAGCAC | 55008 |
| rs28368987 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88379734 | TATATATAATATATA[A/T]ATATATAAATATATA | 55008 |
| rs28380626 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HERC6 | GRCh38.p7 | 4:88382653 | TGTTTTTAAGAGTCA[A/G]TTTGAACATTCAGCA | 55008 |
| rs28396131 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | HERC6, LOC102723458 | GRCh38.p7 | 4:88422159 | ACTGTCTTTGATGTA[C/G/T]AGAAATGCAGTAATT | 55008 |
| rs28409361 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88379717 | AATATATAATATATA[A/T]ATATATATAATATAT | 55008 |
| rs28418714 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88380357 | TATATAATATAAATA[A/T]ATATATAATATATAA | 55008 |
| rs28435459 | snp | A/C/T | 0.0490646 | 0.148751 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HERC6 | GRCh38.p7 | 4:88390842 | CTGGGGAAGTAACAG[A/C/T]GCCGGGCAGCTGGCC | 55008 |
| rs28442062 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88407067 | CCCAGCCTCTTTTTT[A/T]AATTTTTATTATTTT | 55008 |
| rs28445810 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88379719 | TATATAATATATAAA[A/T]ATATATAATATATAA | 55008 |
| rs28490411 | snp | A/G/T | 0.0193847 | 0.0965802 | upstream-variant-2KB | HERC6 | GRCh38.p7 | 4:88377346 | CCTCTAGCCTCTGCT[A/G/T]TACTGTCACCACATT | 55008 |
| rs28507512 | snp | A/C | 0.00835141 | 0.0640778 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HERC6 | GRCh38.p7 | 4:88378808 | GGGCGGGTTGAAGAC[A/C]GGGTGAGTCTCTTGA | 55008 |
| rs28524752 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88379704 | TATATAATATATAAA[A/T]ATATAATATATAAAT | 55008 |
| rs28532472 | snp | C/T | 0.185788 | 0.241613 | intron-variant | HERC6 | GRCh38.p7 | 4:88384132 | GGAATTCAGTTGTCA[C/T]TAAGATAGACCACCC | 55008 |
| rs28548153 | snp | A/G | 0.119978 | 0.213528 | intron-variant | HERC6 | GRCh38.p7 | 4:88392466 | AAGCACTGGGATTAC[A/G]GGTGTGAGACACCAT | 55008 |
| rs28553877 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88379702 | AATATATAATATATA[A/T]ATATATAATATATAA | 55008 |
| rs28558536 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88379695 | ATATACAAATATATA[A/T]TATATAAATATATAA | 55008 |
| rs28581211 | snp | A/T | | | intron-variant | HERC6 | GRCh38.p7 | 4:88380374 | TATATAATATATAAA[A/T]ATATATATATAATAT | 55008 |